Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
Int J Cardiol ; 392: 131253, 2023 Dec 01.
Article in English | MEDLINE | ID: mdl-37579850

ABSTRACT

OBJECTIVES: There is limited data regarding the impact of exercise on phenotypic expression in hypertrophic cardiomyopathy (HCM). We aimed to investigate whether such an association exists in a cohort of genotype-positive HCM patients. METHODS: In this cross-sectional study of genotype-positive HCM families, we used structured questionnaires to obtain data regarding intensity and duration of exercise of participants starting at the age of 10, as well as data regarding exercise recommendations and their impact on quality of life (QOL). The association of cumulative metabolic-equivalent hours of exercise at different ages with different measures of phenotypic expression (maximal wall thickness, left atrial diameter, extent of late gadolinium enhancement) was analyzed. RESULTS: The study included 109 patients from 55 families, including 43 male (39%) and 90 (83%) phenotype-positive. No association was identified between exercise duration or intensity with any of the phenotypic markers with the exception of greater cumulative exercise associated with younger age at presentation. Similar results were obtained when analysis was limited to exercise until the age of 20, until the age of 30 or only after 30. Among phenotype-positive patients, 89% recalled receiving recommendations regarding exercise restriction, 29% noted reduction in exercise level following such recommendations and 25% noted this having a significant impact on their QOL. CONCLUSION: We found no association between exercise intensity or duration and phenotypic expression in genotype-positive HCM patients. These findings are important for physician-patient discussions and support the recent trend towards more permissive exercise restrictions in HCM.

3.
Expert Opin Investig Drugs ; 17(6): 827-43, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18491985

ABSTRACT

BACKGROUND: Mood disorders are associated with decrements in cognitive function, which are insufficiently treated with contemporary pharmacotherapies. OBJECTIVES: To evaluate the putative neurotherapeutic effects of the mitochondrial cofactors, L-carnitine, acetyl-L-carnitine, and alpha-lipoic acid; and to provide a rationale for investigating their efficacy in the treatment of neurocognitive deficits associated with mood disorders. METHODS: A PubMed search of English-language articles published between January 1966 and March 2007 was conducted using the search terms carnitine and lipoic acid. RESULTS: L-carnitine and alpha-lipoic acid may offer neurotherapeutic effects (e.g., neurocognitive enhancement) via disparate mechanisms including antioxidant, anti-inflammatory, and metabolic regulation. Preliminary controlled trials in depressed geriatric populations also suggest an antidepressant effect with acetyl-L-carnitine. CONCLUSIONS: L-carnitine and alpha-lipoic acid are pleiotropic agents capable of offering neuroprotective and possibly cognitive-enhancing effects for neuropsychiatric disorders in which cognitive deficits are an integral feature.


Subject(s)
Acetylcarnitine/therapeutic use , Cognition Disorders/drug therapy , Mood Disorders/drug therapy , Neuroprotective Agents/therapeutic use , Psychotropic Drugs/therapeutic use , Thioctic Acid/therapeutic use , Acetylcarnitine/pharmacology , Aged , Animals , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Antioxidants/pharmacology , Antioxidants/therapeutic use , Carnitine/pharmacology , Carnitine/therapeutic use , Clinical Trials as Topic/statistics & numerical data , Cognition Disorders/etiology , Cognition Disorders/metabolism , Drug Evaluation, Preclinical , Energy Metabolism/drug effects , Female , Humans , Immunologic Factors/pharmacology , Immunologic Factors/therapeutic use , Male , Mice , Middle Aged , Mitochondria/drug effects , Mood Disorders/metabolism , Mood Disorders/psychology , Neurodegenerative Diseases/drug therapy , Neurodegenerative Diseases/psychology , Neuroprotective Agents/pharmacology , Oxidative Stress/drug effects , Psychotropic Drugs/pharmacology , Rats , Rats, Wistar
SELECTION OF CITATIONS
SEARCH DETAIL
...